OTC Medication Information: DYNAMO DELAY Black Label

DYNAMO DELAY BLACK LABEL- lidocaine spray
Momentum Management LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Lidocaine USP 13%

(approximately 10 mg per spray)

Purpose

Topical Anesthetic

Uses

  • for temporary male genital desensitization, helping to slow the onset of ejaculation
  • helps in temporarily prolonging the time until ejaculation
  • for reducing oversensitivity in the male in advance of intercourse

Warnings

For external use onl

When using this product

avoid contact with the eyes

Stop use and ask a doctor if:

this product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision.
you or your partner develop a rash or irritation, such as burning or itching.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

  • apply 3 or more sprays, not to exceed 10, to head and shaft of penis before intercourse, or use as directed by a doctor.
  • wash product off after intercourse

Inactive Ingredients

Isopropyl Palmitate, SD Alcohol 40B, Stearic Acid

Questions?

310 446 1632 Monday — Friday 9am-5pm(PST)

Manufactured for

Momentum Management LLC

1206 W Jon St

Torrance, CA 90502

Principal Display Panel

Last Longer!

Prolong Your Pleasure!

DYNAMO DELAY

NDC 69664-002-01

Lidocaine USP 13%

(approximately 10mg per spray)

150+ sprays per bottle

Convenient pocket size

Helps in temporarily prolonging the time until ejaculation

Black Label Edition

1/2 fl oz (15mL)

Made in the USA

Bottle Label
(click image for full-size original)
Outer Box
(click image for full-size original)
DYNAMO DELAY BLACK LABEL
lidocaine spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69664-002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE (LIDOCAINE) LIDOCAINE 10 mg in 0.08 mL
Inactive Ingredients
Ingredient Name Strength
ISOPROPYL PALMITATE
STEARIC ACID
ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69664-002-01 1 BOTTLE, SPRAY in 1 BOX contains a BOTTLE, SPRAY
1 15 mL in 1 BOTTLE, SPRAY This package is contained within the BOX (69664-002-01)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part348 01/01/2018
Labeler — Momentum Management LLC (828734397)
Establishment
Name Address ID/FEI Operations
Westwood Laboratories Inc 832280635 manufacture (69664-002)

Revised: 01/2020 Momentum Management LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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